Gene-specific Copy Number Variation Probe-MEGF10
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| Catalog: |
CNVFP-MEGF10-11299 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (MEGF10). The product usually consists of a combination of reagents, which consists of a probe with a selected dye color and a hybridization reagent. We provide CNV FISH Probes with a variety of dye color combinations to meet various challenges. Probe products not only provide some classic color combinations but also provide customized probe services. |
| Application: |
MEGF10 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to MEGF10 genes. This product achieves the purpose of detection by hybridizing with the MEGF10 gene. Due to this design method, our probe products can detect the amplification and deletion of target genes on chromosomes through FISH. |
| Category: |
Copy Number Variation |
| Probe Kits Volume (µL): |
40 μL |
| Quantity: |
20 Tests |
| Hybridization Solution (µL): |
200 μL |
| Turnaround Time: |
7-10 Business Days |
| Shipping Time: |
1-2 Day Expedited Shipping |
| Storage Conditions: |
Store at -20℃ and avoid light; |
| Shipping Conditions: |
-20℃ |
Gene Details
| Gene Name |
Multiple EGF Like Domains 10 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the multiple epidermal growth factor-like domains protein family. The encoded protein plays a role in cell adhesion, motility and proliferation, and is a critical mediator of apoptotic cell phagocytosis as well as amyloid-beta peptide uptake in the brain. Expression of this gene may be associated with schizophrenia, and mutations in this gene are a cause of early-onset myopathy, areflexia, respiratory distress, and dysphagia (EMARDD) as well as congenital myopathy with minicores. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Apr 2012] |
| Gene Symbol |
MEGF10 |
| Location |
5q23.2 |
| Chromosome |
Chromosome5 |
| Coordinates |
This gene maps to 126626455-126796910 in GRCh37 coordinates. |
| Species |
Human |
Dye Colors:
OR
RE
GO
GR
AQ
Order Sheet
| Number |
Dye Color |
Order Name |
Absorbance Maximum |
Emission Maximum |
Add to Cart |
| 1 |
OR
|
CNVFP-MEGF10-11299-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-MEGF10-11299-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-MEGF10-11299-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-MEGF10-11299-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-MEGF10-11299-AQ |
467nm |
418nm |
|
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